Label: CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30% liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-9036-9 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 17, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 9036-9 CANTHARIDIN 1% / PODOPHYLLUM RESIN USP 5% / SALICYLIC ACID USP 30%. Liquid 15 gm
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INGREDIENTS AND APPEARANCE
CANTHARIDIN 1% / PODOPHYLLUM RESIN 5% / SALICYLIC ACID 30%
cantharidin 1% / podophyllum resin 5% / salicylic acid 30% liquidProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-9036 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 30 g in 100 g CANTHARIDIN (UNII: IGL471WQ8P) (CANTHARIDIN - UNII:IGL471WQ8P) CANTHARIDIN 1 g in 100 g PODOPHYLLUM RESIN (UNII: 16902YVY2B) (PODOPHYLLUM RESIN - UNII:16902YVY2B) PODOPHYLLUM RESIN 5 g in 100 g Product Characteristics Color brown (traslucent) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-9036-9 15 g in 1 VIAL; Type 0: Not a Combination Product 05/17/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/17/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-9036)
